Join us on February 17, 2011, at 11 a.m. ET to learn more about why cleaning validation issues have ranked in the top five for FDA warning letters. With the advent of new online technologies and changes in the regulatory approach to validation, traditional cleaning validation can move more towards a mode of cleaning verification. This presentation will describe the whys and wherefores of cleaning validation with recommendations of procedures and interpretation. Data on a new approach for screening and specific analysis using charged aerosol detection with FIA and UHPLC will be presented. Live Q+A will follow-bring your questions for the experts.